CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 46 enrolled
Drug / intervention
RAD001 +1 moredrug
Likely dose
RAD001 5.0 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02991807
NCT02991807Phase 2Completed

A Randomized Double-Blind Controlled Trial of Everolimus in Individuals With PTEN Mutations (RAD001XUS257T)

Boston Children's Hospital·interventional·Posted Dec 14, 2016·Updated Feb 17, 2025

In Brief

A Phase 2 clinical trial evaluating RAD001 and Placebo for PTEN Gene Mutation and PTEN Hamartoma Tumor Syndrome. Completed, enrolled 46 participants across 3 sites.

Detailed Summary

Phosphatase and TENsin homolog (PTEN) gene germline mutations are associated with a spectrum of clinical manifestations characterized by neurocognitive deficits, intellectual disability, autism symptomatology, skin lesions, macrocephaly, hamartomatous overgrowth of tissues, and an increased risk of cancers. Investigators are conducting research to evaluate the potential safety and efficacy of RAD001 (everolimus) in this patient population, and the potential neurocognitive benefits from treatment with RAD001 or placebo for a six month period. The investigators hope this trial will lead to a better understanding of PTEN and to new forms of treatment that may benefit children and adults with PTEN in the future.

Study Details

Timeline

Phase 2CompletedFinished
2017201820192020202120222023202420252026
First PostedDec 14, 2016
Enrollment StartJun 12, 2017
Primary CompletionFeb 18, 2021
Study CompletionDec 22, 2021
TodayJul 2, 2026
Enrollment to primary: 3.7 yearsPosted 9.5 years ago

Interventions

RAD001drug

RAD001 is formulated as tablets of 5.0 mg strength, blister-packed under aluminum foil in units of 10 tablets and dosed on a regular basis. RAD001 tablets should be opened only at the time of administration as drug is both hygroscopic and light-sensitive. Patients will be instructed to take 4.5 mg/m2 of RAD001 orally with a glass of water at regular intervals at the same time (delete: each day) in the morning after a light, nonfat breakfast.

Placebodrug

Matching placebo will be provided as a matching tablet and will also be blister packed under aluminum foil in units of 10. Matching placebo tablets should be opened only at the time of administration as drug is both hygroscopic and light-sensitive. Patients will be instructed to take 4.5 mg/m2 of the matching placebo orally with a glass of water at regular intervals at the same time (delete: each day) in the morning after a light, nonfat breakfast.